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4-(TERT-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID PINACOL ESTER is a boronic acid derivative compound characterized by the chemical formula C16H26BNO4S. It is recognized for its role in organic synthesis, particularly as a reagent in Suzuki-Miyaura coupling reactions, which are pivotal for the formation of carbon-carbon bonds in organic molecules. 4-(TERT-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID PINACOL ESTER is distinguished by its selective reactivity with a range of organic substrates, offering versatility in the construction of intricate molecular structures. The pinacol ester group further enhances its stability and solubility in organic solvents, making it an indispensable tool for synthetic chemists in the development of innovative pharmaceuticals, agrochemicals, and materials.

648905-63-9

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648905-63-9 Usage

Uses

Used in Organic Synthesis:
4-(TERT-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID PINACOL ESTER is used as a reagent for Suzuki-Miyaura coupling reactions, which are essential for the formation of carbon-carbon bonds in organic molecules. Its selective reactivity with various organic substrates makes it a versatile tool in the synthesis of complex molecular structures.
Used in Pharmaceutical Development:
In the Pharmaceutical Industry, 4-(TERT-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID PINACOL ESTER is used as a key intermediate in the synthesis of new pharmaceuticals. Its stability and solubility in organic solvents facilitate the development of novel drug candidates with improved efficacy and reduced side effects.
Used in Agrochemical Synthesis:
4-(TERT-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID PINACOL ESTER is utilized as a reagent in the synthesis of agrochemicals, contributing to the development of new pesticides and herbicides with enhanced performance and selectivity.
Used in Material Science:
In the Material Science field, 4-(TERT-BUTYLAMINO)SULFONYLPHENYLBORONIC ACID PINACOL ESTER is employed in the synthesis of advanced materials, such as polymers and composites, with tailored properties for specific applications, including electronics, coatings, and adhesives.

Check Digit Verification of cas no

The CAS Registry Mumber 648905-63-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,8,9,0 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 648905-63:
(8*6)+(7*4)+(6*8)+(5*9)+(4*0)+(3*5)+(2*6)+(1*3)=199
199 % 10 = 9
So 648905-63-9 is a valid CAS Registry Number.

648905-63-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 4-(tert-Butylamino)sulfonylphenylboronic acid pinacol ester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:648905-63-9 SDS

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